A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149727



Internal ID21449694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92545300..92545300hg38UCSC Ensembl
chr7:92174614..92174614hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640648
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149727
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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